94236-21-2

Basic information

• Product Name: 1-broMo-2-((MethoxyMethoxy)Methyl)benzene
• Synonyms: 1-broMo-2-((MethoxyMethoxy)Methyl)benzene
• CAS NO: 94236-21-2
• Molecular Formula: C₉H₁₁BrO₂
• Molecular Weight: 231.08644
• Mol File: 94236-21-2.mol
• Article Data: 11

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-broMo-2-((MethoxyMethoxy)Methyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-broMo-2-((MethoxyMethoxy)Methyl)benzene(94236-21-2)
• EPA Substance Registry System: 1-broMo-2-((MethoxyMethoxy)Methyl)benzene(94236-21-2)

Safety Data

• Hazardous Substances Data: 94236-21-2(Hazardous Substances Data)

Usage

Description

1-Bromo-2-((Methoxymethoxy)methyl)benzene is a brominated derivative of benzene with a methoxymethoxy group attached to the second carbon atom. It has the molecular formula C9H11BrO2 and is commonly used as an intermediate in the synthesis of other organic compounds.

Uses

Used in Pharmaceutical Industry:
1-Bromo-2-((Methoxymethoxy)methyl)benzene is used as an intermediate in the synthesis of pharmaceutical compounds for its potential applications in drug development.
Used in Agrochemical Industry:
1-Bromo-2-((Methoxymethoxy)methyl)benzene is used as an intermediate in the synthesis of agrochemical compounds for its potential applications in the development of pesticides and other agricultural products.
Used in Organic Synthesis:
1-Bromo-2-((Methoxymethoxy)methyl)benzene is used as a versatile intermediate in organic synthesis for the preparation of various organic compounds.
It is important to handle this compound with caution and use appropriate safety measures due to its potential hazards. It is a colorless to pale yellow liquid at room temperature and is typically handled and stored under inert gas to prevent degradation.

Upstream product

• 109-87-5 Dimethoxymethane 
• 18982-54-2 o-bromobenzyl alcohol 
• 107-30-2 chloromethyl methyl ether 

Downstream Products

• 18982-54-2 o-bromobenzyl alcohol 
• 19472-74-3 2-(2-bromophenyl)acetonitrile 
• 81206-50-0 1-(iodomethyl)-2-bromobenzene 
• 3433-80-5 1-Bromo-2-bromomethyl-benzene 
• 1601478-61-8 4-tolyl-(2-methoxymethoxymethyl)phenyl-dimethylsilane 
• 1601478-78-7 4-acetylphenyl-2-methoxymethoxymethylphenyl-dimethylsilane 
• 1380233-28-2 C₁₃H₁₇F₃OSi 
• 1380233-10-2 (E)-[2-{(methoxymethoxy)methyl}phenyl]dimethyl(4,4,4-trifluorobut-1-en-1-yl)silane 
• 1380232-83-6 allyl[2-{(methoxymethoxy)methyl}phenyl]dimethylsilane 
• 59184-20-2 2-bromo-(trimethylsilyloxymethyl)benzene 
• 82466-12-4 2-bromobenzyl acetate 
• 1075740-99-6 1-[1-(4-bromophenyl)-2-nitroethyl]-2-[(methoxymethoxy)methyl]benzene 
• 1140738-70-0 2-(2-methoxymethoxymethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 1082389-26-1 1-methoxy-2-[1-{2-(methoxymethoxy)phenyl}-2-nitroethyl]benzene 

Relevant articles and documents

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[InCl4]: An efficient catalyst-medium for alkoxymethylation of alcohols and their interconversion to acetates and TMS-ethers

A simple, green and chemoselective method for methoxymethylation and ethoxymethylation of primary and secondary alcohols using a Lewis acidic room temperature ionic liquid, [C4mim][InCl4], as catalyst and reaction medium under ambient temperature, microwave and ultrasonic irradiations is reported. In this catalytic system, the corresponding MOM-and EOM-ethers are obtained in excellent yields and in short reaction times. Furthermore, this catalytic system was used for mild and efficient transformations of these protected alcohols to their corresponding acetates and trimethylsilyl ethers under thermal conditions and microwave and ultrasonic irradiations.